Processes for removing carbon disulfide from symmetrical and asymmetrical sulfide product streams

ABSTRACT

Processes for removing carbon disulfide from product streams containing a sulfide compound are performed by contacting the product stream with an alkanolamine and converting the carbon disulfide to a higher boiling point product, thereby reducing or eliminating carbon disulfide from the product stream. Subsequent removal of the higher boiling point product via distillation can lead to a purified sulfide stream with high purity.

FIELD OF THE INVENTION

Sulfide compounds have wide industrial application, for instance as gasodorants, and in paper production from wood products. Impuritiescommonly present in sulfide product streams can result in unwantedreactivity during their intended use, as well as cause corrosion in therelated machinery and equipment. The present disclosure generallyrelates to the removal of impurities such as carbon disulfide (CS₂) fromproduct streams containing sulfide compounds.

BACKGROUND OF THE INVENTION

Product streams containing sulfide compounds also can contain impuritiesthat are difficult to remove from the product streams directly.Impurities that have similar physical or chemical attributes to those ofother components in the product stream, including the sulfide compounditself, can be particularly difficult to separate. Moreover, removal ofimpurities beyond a certain degree may require conditions that can becommercially impractical for large-scale production operations. Thus, itwould be beneficial to develop processes that can improve the efficiencyand effectiveness of removing impurities from product streams containingsulfide compounds. Accordingly, it is to these ends that the presentinvention is generally directed.

SUMMARY OF THE INVENTION

This summary is provided to introduce a selection of concepts in asimplified form that are further described below in the detaileddescription. This summary is not intended to identify required oressential features of the claimed subject matter. Nor is this summaryintended to be used to limit the scope of the claimed subject matter.

The invention disclosed herein generally relates to processes forpurifying a product stream containing a sulfide compound and CS₂. Theprocesses can comprise (i) contacting the product stream with analkanolamine to convert at least a portion of the CS₂ to a higherboiling point product, and (ii) removing at least a portion of thehigher boiling point product from the product stream to form a purifiedsulfide stream. These processes can be applied to product streamscontaining a sulfide compound having formula (I):R¹—S—R²  (I).

Generally, R¹ and R² independently can be a C₁ to C₁₈ substituted orunsubstituted, cycloalkyl group or linear or branched alkyl group. Incertain aspects, the sulfide compound can be dimethyl sulfide or methylethyl sulfide.

Various alkanolamines can be used in the disclosed processes, such asβ-hydroxy amines. In some aspects, the alkanolamine can have aheteroatom-containing linking group between the hydroxy and aminegroups.

Processes disclosed herein can form purified sulfide streams having lowlevels of carbon disulfide. For instance, the processes disclosed hereincan have a ratio of the concentration of CS₂ present in the productstream prior to step (i) to the concentration of CS₂ present in thepurified sulfide stream of at least about 100:1—thus, a 100-foldreduction in the CS₂ concentration.

Optionally, the processes disclosed herein can further comprise thesteps of determining a concentration of the CS₂ in the product stream,and adjusting an amount of the alkanolamine contacted with the productstream based on the concentration of the CS₂ in the product stream.Similarly, the processes disclosed herein can further comprise the stepsof determining a concentration of the CS₂ in the purified sulfidestream, and adjusting an amount of the alkanolamine contacted with theproduct stream based on the concentration of the CS₂ in the purifiedsulfide stream.

Both the foregoing summary and the following detailed descriptionprovide examples and are explanatory only. Accordingly, the foregoingsummary and the following detailed description should not be consideredto be restrictive. Further, features or variations may be provided inaddition to those set forth herein. For example, certain aspects andembodiments may be directed to various feature combinations andsub-combinations described in the detailed description.

BRIEF DESCRIPTION OF THE FIGURES

The following figures form part of the present specification and areincluded to further demonstrate certain aspects of the presentinvention. The invention may be better understood by reference to one ormore of these figures in combination with the detailed description andexamples.

FIG. 1 illustrates a carbon disulfide removal system consistent with anaspect of the present invention.

FIG. 2 illustrates a mercaptan and sulfide production system consistentwith another aspect of the present invention.

DEFINITIONS

To define more clearly the terms used herein, the following definitionsare provided. Unless otherwise indicated, the following definitions areapplicable to this disclosure. If a term is used in this disclosure butis not specifically defined herein, the definition from the IUPACCompendium of Chemical Terminology, 2^(nd) Ed (1997), can be applied, aslong as that definition does not conflict with any other disclosure ordefinition applied herein, or render indefinite or non-enabled any claimto which that definition can be applied. To the extent that anydefinition or usage provided by any document incorporated herein byreference conflicts with the definition or usage provided herein, thedefinition or usage provided herein controls.

Herein, features of the subject matter can be described such that,within particular aspects and/or embodiments, a combination of differentfeatures can be envisioned. For each and every aspect, and/orembodiment, and/or feature disclosed herein, all combinations that donot detrimentally affect the designs, processes, and/or methodsdescribed herein are contemplated with or without explicit descriptionof the particular combination.

Additionally, unless explicitly recited otherwise, any aspect, and/orembodiment, and/or feature disclosed herein can be combined to describeinventive features consistent with the present disclosure.

While compositions and processes are described in terms of “comprising”various components or steps, the compositions and methods also can“consist essentially of” or “consist of” the various components orsteps, unless specifically stated otherwise.

The terms “a,” “an,” and “the” are intended to include pluralalternatives, e.g., at least one, unless otherwise specified. Forinstance, the disclosure of “a higher boiling point product” and “analkanolamine” is meant to encompass one, or mixtures or combinations ofmore than one, higher boiling point product and alkanolamine,respectively, unless otherwise specified.

All “ppm” quantities disclosed herein refer to ppm by weight, unlessspecifically stated otherwise.

For any particular compound or group disclosed herein, any name orstructure presented is intended to encompass all conformational isomers,regioisomers, and stereoisomers that can arise from a particular set ofsubstituents, unless otherwise specified. For example, a generalreference to pentane includes n-pentane, 2-methyl-butane, and2,2-dimethylpropane, and a general reference to a butyl group includesan n-butyl group, a sec-butyl group, an iso-butyl group, and a t-butylgroup. The name or structure also encompasses all enantiomers,diastereomers, and other optical isomers whether in enantiomeric orracemic forms, as well as mixtures of stereoisomers, as would berecognized by a skilled artisan, unless otherwise specified.

The term “substituted” when used to describe a group, for example, whenreferring to a substituted analog of a particular group, is intended todescribe any non-hydrogen moiety that formally replaces a hydrogen inthat group and is intended to be non-limiting. A group or groups canalso be referred to herein as “unsubstituted” or by equivalent termssuch as “non-substituted,” which refers to the original group in which anon-hydrogen moiety does not replace a hydrogen within that group.Unless otherwise specified, “substituted” is intended to be non-limitingand include inorganic substituents or organic substituents as understoodby one of ordinary skill in the art.

The term “hydrocarbon” whenever used in this specification and claimsrefers to a compound containing only carbon and hydrogen. Otheridentifiers can be utilized to indicate the presence of particulargroups in the hydrocarbon (e.g., halogenated hydrocarbon indicates thepresence of one or more halogen atoms replacing an equivalent number ofhydrogen atoms in the hydrocarbon). The term “hydrocarbyl group” is usedherein in accordance with the definition specified by IUPAC: a univalentgroup formed by removing a hydrogen atom from a hydrocarbon (that is, agroup containing only carbon and hydrogen). Non-limiting examples ofhydrocarbyl groups include alkyl, alkenyl, aryl, and aralkyl groups,amongst other groups.

As used herein, the term “alkanolamine” refers to a compound having botha hydroxy group and an amine group. The amine group can be a primary,secondary, or tertiary amine group. Alkanolamine encompassesmonoalkanolamines (one hydroxy group), dialkanolamines (two hydroxygroups), and trialkanolamines (three hydroxy groups). Additionally, thealkanolamine can contain, in some aspects, a heteroatom-containinglinking group between the amine and hydroxy group(s). The alkanolaminecan be linear or branched, and substituted or unsubstituted, as would berecognized by a skilled artisan.

The terms “contacting” and “combining” are used herein to describemethods and processes in which the materials or components are contactedor combined together in any order, in any manner, and for any length oftime, unless otherwise specified. For example, the materials orcomponents can be blended, mixed, slurried, dissolved, reacted, treated,compounded, impregnated, or otherwise contacted or combined in someother manner or by any suitable method or technique.

Several types of ranges are disclosed in the present invention. When arange of any type is disclosed or claimed, the intent is to disclose orclaim individually each possible number that such a range couldreasonably encompass, including end points of the range as well as anysub-ranges and combinations of sub-ranges encompassed therein. Forexample, when a chemical moiety having a certain number of carbon atomsis disclosed or claimed, the intent is to disclose or claim individuallyevery possible number that such a range could encompass, consistent withthe disclosure herein. For example, the disclosure that a moiety is a C₁to C₁₂ hydrocarbyl group, or in alternative language, a hydrocarbylgroup having from 1 to 12 carbon atoms, as used herein, refers to amoiety that can have 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbonatoms, as well as any range between these two numbers (for example, a C₂to C₆ hydrocarbyl group), and also including any combination of rangesbetween these two numbers (for example, a C₂ to C₄ and a C₈ to C₁₂hydrocarbyl group).

Similarly, another representative example follows for the molar ratio ofalkanolamine:CS₂ employed in aspects of step (i) of the disclosedprocesses. By a disclosure that the molar ratio of alkanolamine:CS₂ canbe in a range from about 1:1 to about 6:1, the intent is to recite thatthe ratio of alkanolamine:CS₂ can be any ratio in the range and, forexample, can be equal to about 1:1, about 1.5:1, about 2:1, about 3:1,about 4:1, about 5:1, or about 6:1. Additionally, the ratio ofalkanolamine:CS₂ can be within any range from about 1:1 to about 6:1(for example, from about 2:1 to about 6:1), and this also includes anycombination of ranges between about 1:1 and about 6:1 (for example, thealkanolamine:CS₂ ratio can be in a range from about 3:1 to about 4:1, orfrom about 5:1 to about 6:1). Further, in all instances, where “about” aparticular value is disclosed, then that value itself is disclosed.Thus, the disclosure that the ratio of alkanolamine:CS₂ can be fromabout 1:1 to about 6:1 also discloses a ratio from 1:1 to 6:1 (forexample, from 2:1 to 6:1), and this also includes any combination ofranges between 1:1 and 6:1 (for example, the alkanolamine:CS₂ ratio canbe in a range from 3:1 to 4:1, or from 5:1 to 6:1). Likewise, all otherranges disclosed herein should be interpreted in a manner similar tothese examples.

The term “about” means that amounts, sizes, formulations, parameters,and other quantities and characteristics are not and need not be exact,but can be approximate and/or larger or smaller, as desired, reflectingtolerances, conversion factors, rounding off, measurement errors, andthe like, and other factors known to those of skill in the art. Ingeneral, an amount, size, formulation, parameter or other quantity orcharacteristic is “about” or “approximate” whether or not expresslystated to be such. The term “about” also encompasses amounts that differdue to different equilibrium conditions for a composition resulting froma particular initial mixture. Whether or not modified by the term“about,” the claims include equivalents to the quantities. The term“about” can mean within 10% of the reported numerical value, preferablywithin 5% of the reported numerical value.

Although any methods and materials similar or equivalent to thosedescribed herein can be used in the practice or testing of theinvention, the typical methods and materials are herein described.

All publications and patents mentioned herein are incorporated herein byreference for the purpose of describing and disclosing, for example, theconstructs and methodologies that are described in the publications,which might be used in connection with the presently describedinvention.

DETAILED DESCRIPTION OF THE INVENTION

Many product streams containing sulfide compounds also containimpurities that are both difficult to remove and limit the ability ofthe sulfide product stream to be used in a variety of desirable end-useapplications. For instance, dimethyl sulfide product streams oftencontain 2000-4000 ppm by weight of carbon disulfide (CS₂). While thepurity of the dimethyl sulfide in the product stream is very high (e.g.,greater than 98 wt. %, and often greater than 99 wt. %), ppm amounts ofcarbon disulfide present in the dimethyl sulfide product stream canprevent it from being used in end-use applications that requiresubstantially “pure” dimethyl sulfide, generally requiring ppm amountsof carbon disulfide of less than 100 ppm, and in some cases, less than20 ppm. For example, a dimethyl sulfide product with less than 1 ppm CS₂may be preferred for use in ethylene plants and as a reagent forsynthesizing dimethyl sulfoxide (DMSO). However, removal of carbondisulfide (CS₂) from dimethyl sulfide using conventional separationstechniques, such as distillation, cannot approach the very low ppmlevels of carbon disulfide needed to produce substantially pure dimethylsulfide. Thus, alternative means for eliminating difficult-to-removeimpurities from such sulfide product streams are needed.

Accordingly, disclosed herein are alternative processes for purifyingproduct streams comprising (or consisting essentially of, or consistingof) a sulfide compound and carbon disulfide (CS₂). Such processes cancomprise (or consist essentially of, or consist of) (i) contacting theproduct stream with an alkanolamine to convert at least a portion of thecarbon disulfide to a higher boiling point product, and (ii) removing atleast a portion of the higher boiling point product from the productstream to form a purified sulfide stream. Generally, the features of theprocesses (e.g., the components and/or features of the product stream,the alkanolamine, the components and/or features of the purified sulfidestream, and the process conditions under which the product stream andalkanolamine are contacted, among others) are independently describedherein, and these features can be combined in any combination to furtherdescribe the disclosed purification processes.

The amount of the sulfide compound present in the product stream is notparticularly limited, although the sulfide compound generallyconstitutes the vast majority of the product stream, for instance, atleast about 80 wt. %, at least about 85 wt. %, or at least about 90 wt.%, and more often, the product stream contains at least about 95 wt. %,at least about 98 wt. %, at least about 99 wt. %, or at least about 99.9wt. %, of the sulfide compound.

Representative ranges for the amount of the sulfide compound in theproduct stream can include from about 90 wt. % to about 99.99 wt. %,from about 95 wt. % to about 99.99 wt. %, from about 98 wt. % to about99.9 wt. %, or from about 99 wt. % to about 99.9 wt. %. Thus, theproduct stream can be a relatively pure sulfide product streamcontaining only trace amounts of certain impurities, and the impuritiescan be difficult to remove by conventional purification processes.

In addition to the sulfide compound, the product stream can contain anunacceptably high amount of carbon disulfide. In some aspects, theproduct stream prior to step (i) can contain from about 100 ppm to about10,000 ppm (by weight) of carbon disulfide, such as from about 250 ppmto about 5000 ppm, from about 500 ppm to about 10,000 ppm, from about1000 ppm to 5000 ppm, or from about 2000 ppm to about 4000 ppm, althoughnot limited thereto. In other aspects, the amount of carbon disulfidepresent in the product stream can be at least about 100 ppm, at leastabout 250 ppm, at least about 500 ppm, at least about 1000 ppm, or atleast about 2000 ppm (by weight).

The product stream also can contain additional impurities andby-products from the production of the sulfide compound. Such additionalimpurities can further complicate the purification of the productstream. As an example, the product stream can comprise hydrogen sulfideand/or water prior to step (i). Where present, the product stream cancontain an amount of H₂S in a range from about 1 ppm to about 100 ppm,or from about 5 ppm to about 75 ppm. Similarly, the product stream cancontain an amount of water in a range from about 10 ppm to about 1000ppm, from about 50 ppm to about 500 ppm, or from about 10 ppm to about100 ppm. In certain aspects, the amount of H₂S and/or water in thepurified sulfide stream independently can be unchanged, less than, orgreater than that in the product stream containing the sulfide compound.

In step (i), the product stream can be contacted with an alkanolamine toconvert at least a portion of the CS₂ to a higher boiling point product.Any suitable temperature and pressures conditions can be used for step(i). The temperature is not particularly limited, and generally can beany temperature sufficient and practical for the alkanolamine to reactwith the CS₂ and form a higher boiling point product. For instance, step(i) can be conducted without heating, at ambient temperature. In otheraspects, the temperature of step (i) can be in a range from about 15° C.to about 85° C., from about 20° C. to about 70° C., from about 25° C. toabout 60° C., or from about 30° C. to about 45° C. Similarly, thepressure in step (i) is not particularly limited, but in some aspects,can be such that each component of the product stream remains a liquidat the operating temperature. Thus, step (i) can be conducted at ambientpressure or a pressure of at least 5 psig (34 kPag), at least 10 psig(69 kPag), at least 15 psig (103 kPag), at least 20 psig (138 kPag), atleast 25 psig (172 kPag), at least 30 psig (207 kPag), at least 40 psig(276 kPag), at least 50 psig (345 kPag), at least 60 psig (414 kPag), atleast 80 psig (551 kPag), or at least 100 psig (689 kPag). In someaspects, step (i) can be conducted at a pressure in a range from ambientpressure to about 100 psig (689 kPag), or from about 5 psig (34 kPag) toabout 60 psig (414 kPag).

If desired, a diluent can be used in step (i), such that the productstream is contacted with the alkanolamine in a diluent. Suitablediluents contemplated herein include alcohol, ether, and hydrocarbonsolvents. In certain aspects, the diluent can comprise an alcohol, suchas C₁ to C₃ alcohol (e.g., methanol, ethanol, or isopropanol). Anysuitable amount of the diluent can be used, and when a diluent ispresent, the weight ratio of alkanolamine:diluent can range from about99:1 to about 10:90, from about 95:5 to about 25:75, from about 85:15 toabout 50:50, or from about 90:10 to about 70:30.

Any suitable relative amount of the alkanolamine and carbon disulfidecan be used in step (i). For instance, the molar ratio ofalkanolamine:CS₂ can be in a range from about 1:1 to about 20:1, fromabout 1:1 to about 6:1, from about 1.5:1 to about 10:1, from about 1.5:1to about 5:1, from about 2:1 to about 6:1, or from about 3:1 to about10:1. Often, it can be beneficial to use an excess of the alkanolaminerelative to the amount of carbon disulfide impurity in the productstream.

Similarly, the alkanolamine can be added to the product stream in anysuitable amount relative to the total weight of the product stream. Insome aspects, the amount of the alkanolamine added to the product streamcan be in a range from about 0.01 to about 5 wt. %, from about 0.1 toabout 3 wt. %, from about 0.1 to about 2 wt. %, from about 0.2 to about1 wt. %, from about 0.3 to about 0.9 wt. %, or from about 0.4 to about1.5 wt. %, based on the weight of the product stream.

Optionally, the amount of CS₂ present in the product stream can bemonitored, and the amount of the alkanolamine added to the productstream can be controlled accordingly. For instance, the processesdisclosed herein can further comprise the steps of determining (ormeasuring) the concentration of the CS₂ present in the product stream,and adjusting the amount of alkanolamine contacted with the productstream based on the concentration of CS₂ in the product stream (thedetermined concentration). In such aspects, a target ratio ofalkanolamine:CS₂ can be efficiently maintained to ensure substantiallycomplete conversion of the CS₂ during step (i) of the process,regardless of upward/downward spikes in the concentration of CS₂ in theproduct stream. This methodology also can reduce costs by avoidingexcess addition of the alkanolamine, when it is not needed.

Step (i) can be conducted for any suitable period of time, generally fora time period sufficient for substantially all of the CS₂ to beconverted to the higher boiling point product. Although the particulartime can vary based on temperature and alkanolamine:CS₂ molar ratio,among other variables, step (i) often can be conducted for a time periodin a range from about 0.5 min to about 24 hr, from about 1 min to about24 hr, from about 2 min to about 12 hr, from about 2 min to about 2 hr,from about 2 min to about 30 min, or from about 5 min to about 1 hr, andthe like. To improve the contact between the alkanolamine and the CS₂components, which are present in small amounts in step (i), the mixtureof the product stream (containing CS₂) and the alkanolamine can bevigorously agitated in step (i).

The conditions and components disclosed herein can be combined in anymanner to effectuate an efficient conversion of at least a portion ofthe CS₂ present in the product stream. Generally, at least about 40 wt.% of the CS₂ in the product stream is converted to a higher boilingpoint product, and more often, at least about 50 wt. %, at least about60 wt. %, at least about 70 wt. %, at least about 80 wt. %, at leastabout 85 wt. %, at least about 90 wt. %, at least about 95 wt. %, or atleast about 98 wt. %, and in some instances, at least about 99 wt. %, atleast about 99.9 wt. %, or at least about 99.99 wt. %. Thus, typicalamounts of the CS₂ in the product stream that are converted into ahigher boiling point product can range from about 60 wt. % to about99.99 wt. %, from about 90 wt. % to about 99.9 wt. %, or from about 98wt. % to about 99.99 wt. %.

The higher boiling point product (or products) formed in step (i) can bedependent on the structure of the alkanolamine and the reaction thattakes place with CS₂. In some aspects, the higher boiling point productcan comprise a cyclic product, while in other aspects, the higherboiling point product can comprise a heterocyclic organic compound,e.g., with oxygen, nitrogen, sulfur, or any combination thereof, in thering. Regardless of the structure of the higher boiling point product(or products), beneficially, the “higher boiling point product” has ahigher boiling point (at 1 atm, normal boiling point) than that of CS₂(which has a normal boiling point of ˜46-47° C.). Additionally, thehigher boiling point product can have a higher boiling point (normalboiling point) than that of the sulfide compound in the product stream(e.g., dimethyl sulfide has a normal boiling point of ˜35-41° C.). Alarger difference between the respective boiling points of the higherboiling point product (or products) and the sulfide compound in theproduct stream can facilitate easier separation or removal of the higherboiling point product from the product stream in step (ii), e.g., viadistillation. Thus, in certain aspects, the normal boiling point of thehigher boiling point product can be at least about 20° C. greater, atleast about 30° C. greater, at least about 40° C. greater, at leastabout 50° C. greater, at least about 75° C. greater, or at least about100° C. greater, than the normal boiling point of CS₂ and/or the normalboiling point of the sulfide compound.

Additionally, it can be beneficial for the higher boiling point product(or products) to be a liquid (not a solid) and to remain in the liquidstate at a particular set of process conditions, such as at standardtemperature and pressure (STP, 1 atm and 20° C.); additionally oralternatively, a liquid at 0° C. and 2 atm, additionally oralternatively, a liquid at −10° C. and 2 atm.

In addition to a higher boiling point product (or products), theconversion of CS₂ in step (i) also can produce lower boiling pointbyproducts, such as H₂S. However, trace amounts of H₂S resulting fromstep (i) would not be problematic, since H₂S is a gas at STP, andtherefore can be easily removed from the product stream.

As a non-limiting example of step (i) in which the alkanolamine isethanolamine, and the sulfide compound is dimethyl sulfide, step (i) canproduce the products shown in Scheme I below. Several higher boilingpoint products with boiling points much greater than that of both thesulfide compound and CS₂ are produced.

Scheme I. Conversion of CS₂ to various higher boiling point products andbyproducts in a product stream containing dimethyl sulfide.

Thus, the higher boiling point product can comprise a heterocyclicorganic compound. For instance, β-hydroxy amines can form stabile5-membered cyclic products that incorporate both the nitrogen and oxygenof the alkanolamine compound within the ring through sequential additionto the electrophilic carbon of CS₂. The higher boiling point product cancontain oxygen, nitrogen, or sulfur, in any arrangement within the ringof a cyclic product.

Referring now to step (ii), in which at least a portion of the higherboiling point product is removed or separated from the product stream toform the purified sulfide stream. Any suitable technique can be used toremove the higher boiling point product (or products) from the productstream. Such techniques can include filtration, extraction, evaporation,distillation, and the like, or any combination of two or more of thesetechniques. For instance, the higher boiling point product can beremoved from the product stream using distillation to form the purifiedsulfide stream. In such aspects, the product stream containing thesulfide compound can proceed to a distillation kettle where the sulfidecompound can be distilled through a column to an overhead condenser,leaving the higher boiling point product(s) in the refluxingdistillation kettle below. In this manner, the product stream proceedsfrom the distillation kettle through the column, and forms the purifiedsulfide stream, while the higher boiling point product(s) can be removedfrom the product stream and remain in the distillation kettle.

In aspects where step (ii) comprises distillation, the distillation canbe performed at any temperature and pressure conditions suitable for theremoval of the higher boiling point product from the product stream, andto suitably result in a purified sulfide stream. For instance, thedistillation pressure can be in a range from ambient to about 100 psig(689 kPag), from about 20 psig to about 50 psig (138 kPag to 345 kPag),or from about 5 psig to about 30 psig (35 kPag to 207 kPag). Thedistillation temperature (at the top of the column) can be in a rangefrom about 25° C. to about 120° C., from about 35° C. to about 125° C.,from about 65° C. to about 120° C., or from about 85° C. to about 120°C., and can depend on the particular distillation pressure and thespecific sulfide compound in the product stream and the specific higherboiling point product(s).

In an embodiment where step (ii) comprises distillation, the process canoccur in a distillation tower (or distillation column), such as a packedtower. More specifically, the distillation tower can contain packingthat facilitates mass transfer between the vapor and liquid phases inthe distillation tower. In an alternative embodiment, the distillationtower can contain trays to facilitate the separation. As mentionedpreviously, the purified sulfide stream can exit the top of the tower.In an embodiment, the alkanolamine can be added to the distillationtower at a point at or below at least one layer of packing.Alternatively, the alkanolamine can be added continuously to the feed(the impure product stream) to the distillation tower and is mixed intothe feed via an in-line static mixer. In an embodiment, the temperatureat the point of alkanolamine addition is above 37° C.

In an embodiment, the function of the distillation tower is to removeCS₂ impurities from dimethyl sulfide (DMS). In an embodiment, thepurified DMS contains less than 20 ppm by weight CS₂, or alternatively,less than 1 ppm (by weight) CS₂.

In an embodiment, the alkanolamine is ethanolamine (monoethanolamine(MEA)). In another embodiment, the ethanolamine is diethanolamine (DEA).The alkanolamine can be mixed with a solvent before it is added eitherdirectly to the distillation tower or mixed with the distillation towerfeed. Any suitable solvent that is miscible with the alkanolamine may beused. For example, solvents such as water, methanol, isopropanol,acetone, methyl ethyl ketone, or glycerol may be suitable. However, forcertain alkanolamines, such as MEA, certain solvents such as water andmethanol can form azeotropes with DMS or cause unwanted phaseseparations. In an embodiment, the alkanolamine is mixed withisopropanol before being added to the distillation tower or to thedistillation tower feed.

In yet another embodiment, the amount of alkanolamine added (either tothe distillation tower or to the distillation tower feed) is controlledvia a feedback control loop. A carbon disulfide removal system 100 isshown in FIG. 1, in which an alkanolamine feed 102 can be added eitherdirectly to distillation tower 110 via inlet 102A, or alternatively,alkanolamine feed stream 102B can be mixed with impure sulfide productstream 101 to form distillation tower feed stream 105. In instanceswhere the alkanolamine is added to the tower 110 only via inlet 102A,product stream 101 and feed stream 105 are the same.

As shown in FIG. 1, the amount of alkanolamine added to distillationtower 110 can be controlled by measuring the concentration of CS₂ inoverhead stream 155 leaving the distillation tower. In an embodiment,the concentration of CS₂ can be measured using any suitable analyticalinstrument 120, such as online analyzer (e.g., gas chromatograph)equipped with a sulfur chemiluminescence detector. If the measured CS₂concentration is higher than desired, then a feedback control loop usingflow indicator controller 125A will signal for valve 122A to open andmore alkanolamine will be added via inlet 102A, in circumstances wherethe alkanolamine is fed directly to the tower. Moreover, if the measuredCS₂ concentration is lower than desired, then the feedback control loopwill signal for valve 122A to close. In like manner, a similar controlscheme using flow indicator controller 125B and value 122B can be usedif the alkanolamine is mixed with impure sulfide product stream 101. Theamount of alkanolamine added can depend on the flow rate of the impuresulfide product stream 101, as measured by flow indicator 130, and aratio indicator controller 135 can be used to control and optimize theamount of alkanolamine (relative to the sulfide product stream) requiredto achieve the desired concentration of CS₂ in stream 155 leaving thetop of the distillation tower.

If desired, overhead stream 155 can be passed through heat exchanger150, thereby forming purified sulfide stream 165, while some of theoverhead stream 155 can be refluxed to the tower via stream 175. Theheavies stream 145 exits the bottom of the tower and also can be passedthrough heat exchanger 140.

The distillation tower capable of producing a purified sulfide stream,such as a DMS stream containing less than 20 ppm by weight, oralternatively, 1 ppm by weight or less CS₂ can be part of an integratedsystem for producing mercaptans such as methyl mercaptan (MeSH) from thereaction of methanol and H₂S. In addition to producing mercaptans, theprocess can also produce dimethyl sulfide (DMS) and CS₂, as well asother products and byproducts.

As shown in FIG. 2, system 200 can include (but is not limited to) thefollowing: i) a methanol (or other alcohol, such as ethanol) feed stream225; ii) an H₂S feed stream 205; iii) a mercaptan synthesis unit 220;iv) and a product purification and fractionation unit 240 where the MeSHproduct stream 265 is separated from the DMS product stream 275 and ventstream 292. In an embodiment, the mercaptan synthesis unit 220 can be acatalytic flow reactor. In another embodiment, excess (recycle) H₂S 235is separated from reactor effluent 255, and stream 235 can be combinedwith feed inlet 215 to the mercaptan synthesis unit 220. H₂S feed stream205 is passed through compressor 210 prior to entering the mercaptansynthesis unit.

The product purification and fractionation unit 240 can include a phaseeffluent separator and one or more distillation towers. Stream 285 canbe sent to a water purification unit 230 to separate a water stream 295from a methanol recycle stream 245 (which also may contain some H₂S),and stream 245 can be combined with methanol feed stream 225. In anembodiment, DMS product stream 275 containing CS₂ (and other impurities)is produced as an overhead product from the last column in the series ofcolumns in unit 240.

In a further embodiment, the DMS product stream 275 (containing the CS₂impurity) leaving the product purification and fractionation unit 240 ofthe mercaptan and sulfide synthesis system 200 is then further treatedto remove CS₂ via the addition of an alkanolamine. In an embodiment,carbon disulfide removal system 100, as depicted in FIG. 1, isintegrated into system 200 downstream of the product purification andfractionation unit.

In a further embodiment, the highly purified DMS containing less than 20ppm (by weight), less than 10 ppm (by weight), less than 5 ppm (byweight), or less than 1 ppm (by weight) CS₂ has several subsequent uses.In one embodiment, purified DMS containing less than 20 ppm (by weight)can be used in naphtha (or ethane or propane) steam cracking furnacesused for olefins (ethylene) production. The addition of DMS preventscatalytic coking of the furnace tubes used in olefins production andextends the duration between furnace decokes; however, the DMS must below in CS₂ content in order to prevent the CS₂ from accumulating in theC₅+ product fraction. In an alternative embodiment, very high purity DMS(e.g., less than 1 ppm by weight CS₂) can be used as a reagent to makedimethyl sulfoxide (DMSO).

As discussed above, the removal of CS₂ from product streams containing asulfide compound can be problematic due to the components having similarchemical and physical characteristics. Thus, the effectiveness of theremoval step applied directly to CS₂ can be limited, with respect toboth the relative amount of the CS₂ removed (compared to an amount ofCS₂ present in the product stream) and the actual amount of CS₂ removed.Moreover, as the levels of CS₂ in the product stream are reduced, it canbecome increasingly difficult to remove any significant portion of CS₂from the product stream where the chemical and/or physical propertiesare similar. In contrast, in the processes disclosed herein, all orsubstantially all of the CS₂ can be removed from the product stream toform a purified sulfide stream in an efficient manner via the use of anappropriate amount of alkanolamine to react with the CS₂, resulting inhigher boiling point products that are easily removed via conventionaldistillation or other suitable technique.

Generally, at least about 40 wt. % of the higher boiling point product(or products) in the product stream is removed in step (ii), and moreoften, at least about 50 wt. %, at least about 60 wt. %, at least about70 wt. %, at least about 80 wt. %, at least about 85 wt. %, at leastabout 90 wt. %, at least about 95 wt. %, or at least about 98 wt. %, andin some instances, at least about 99 wt. %, at least about 99.9 wt. %,or at least about 99.99 wt. %. Thus, typical amounts of the higherboiling point product that are removed from the product stream can rangefrom about 60 wt. % to about 99.99 wt. %, from about 80 wt. % to about99.99 wt. %, or from about 90 wt. % to about 99.99 wt. %.

As a result, the purified sulfide stream can have exceptional purity ofthe sulfide compound, generally far in excess of methods in which CS₂ isattempted to be removed directly (e.g., by fractional distillation). Theratio of the concentration (ppm by weight) of CS₂ in the product streamprior to step (i) to the concentration (ppm by weight) of CS₂ in thepurified sulfide stream can be at least about 10:1, at least about 25:1,or at least about 100:1, and in some aspects, at least about 250:1, atleast about 500:1, or at least about 1000:1. With regard to the purityof the sulfide compound, the purified sulfide streams formed by theprocesses disclosed herein can contain amounts of CS₂ of less than orequal to about 200 ppm, less than or equal to about 150 ppm, less thanor equal to about 100 ppm, less than or equal to about 75 ppm, less thanor equal to about 50 ppm, less than or equal to about 25 ppm, less thanor equal to about 10 ppm, or less than or equal to about 1 ppm (byweight). Hence, the amount of CS₂ in the purified sulfide stream canrange from about 1 ppm to about 100 ppm, from about 1 ppm to about 50ppm, or from about 1 ppm to about 10 ppm (by weight). With respect tothe overall purity of the sulfide compound in purified sulfide streamformed in step (ii), in certain aspects, the amount of the sulfidecompound in the purified sulfide stream can be at least about 99 wt. %,at least about 99.9 wt. %, at least about 99.99 wt. %, at least about99.995 wt. %, or at least about 99.999 wt. %.

Optionally, the amount of CS₂ present in the purified sulfide stream canbe monitored, and the amount of the alkanolamine added to the productstream can be controlled accordingly. For instance, the processesdisclosed herein can further comprise the steps of determining (ormeasuring) the concentration of the CS₂ present in the purified sulfidestream, and adjusting the amount of alkanolamine contacted with theproduct stream based on the concentration of CS₂ in the purified sulfidestream (the determined concentration). In such aspects, a target ratioof alkanolamine:CS₂ can be efficiently maintained to ensure that lessthan or equal to about 100 ppm, less than or equal to about 25 ppm, lessthan or equal to about 10 ppm, or no measurable amount of the CS₂ ispresent in the purified sulfide stream, regardless of upward/downwardspikes in the concentration of CS₂ in the product stream. SULFIDECOMPOUNDS Generally, the product stream can contain any suitable sulfidecompound in which carbon disulfide also is present as an impurity, andthus may be benefit from the purification processes described herein. Insome aspects, for instance, the product stream can contain a sulfidecompound having formula (I):R¹—S—R²  (I).

In formula (I), R¹ and R² independently can be a C₁ to C₁₈ substitutedor unsubstituted, cycloalkyl group or linear or branched alkyl group. Itis contemplated that R¹ and R² can be the same or different. When R¹ andR² are the same, the sulfide compound is symmetrical, and when R¹ and R²are different, the sulfide compound is asymmetrical. R¹ in formula (I)can be a C₁ to C₁₈ substituted or unsubstituted, cycloalkyl group orlinear or branched alkyl group. In one aspect, for example, R¹ can be aC₁ to C₁₄ substituted or unsubstituted, cycloalkyl group or linear orbranched alkyl group, while in another aspect, R¹ can be a C₁ to C₁₂substituted or unsubstituted, cycloalkyl group or linear or branchedalkyl group, and in yet another aspect, R¹ can be a C₁ to C₈ substitutedor unsubstituted, cycloalkyl group or linear or branched alkyl group.Consistent with aspects of the present invention, R¹ can be a cycloalkylgroup; alternatively, R¹ can be a linear alkyl group; or alternatively,R¹ can be a branched alkyl group. Regardless of whether R¹ is a cyclic,linear, or branched alkyl group, R¹ can be unsubstituted, or can besubstituted with any suitable substituent, any suitable number ofsubstituents, and at any suitable position(s) that conforms to the rulesof chemical valence.

R¹ can be a C₁ to C₁₈ linear or branched alkyl group in certain aspectsof this invention. Thus, R¹ can be a C₁ to C₁₄ linear or branched alkylgroup, a C₁ to C₁₂ linear or branched alkyl group, a C₁ to C₈ linear orbranched alkyl group, or a C₁ to C₆ linear or branched alkyl group.Accordingly, in some aspects, R¹ can be a methyl group, an ethyl group,a propyl group, a butyl group, a pentyl group, a hexyl group, a heptylgroup, an octyl group, a nonyl group, a decyl group, a undecyl group, adodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group,a hexadecyl group, a heptadecyl group, or an octadecyl group; oralternatively, a methyl group, an ethyl group, a propyl group, a butylgroup, a pentyl group, a hexyl group, a heptyl group, an octyl group, adecyl group, or a dodecyl group.

In other aspects, the alkyl group which can be R¹ in formula (I) can bea methyl group, an ethyl group, a n-propyl group, an iso-propyl group, an-butyl group, an iso-butyl group, a sec-butyl group, a tert-butylgroup, a n-pentyl group, an iso-pentyl group, a sec-pentyl group, aneopentyl group, a tert-amyl group, a n-hexyl group, a n-heptyl group, an-octyl group, or a n-dodecyl group; alternatively, a methyl group, anethyl group, or an iso-propyl group; alternatively, a methyl group or anethyl group; alternatively, a methyl group; alternatively, an ethylgroup; alternatively, a n-propyl group; alternatively, an iso-propylgroup; alternatively, a n-butyl group; alternatively, an iso-butylgroup; alternatively, a sec-butyl group; alternatively, a tert-butylgroup; alternatively, a n-pentyl group; alternatively, an iso-pentylgroup; alternatively, a sec-pentyl group; alternatively, a neopentylgroup; alternatively, a tert-amyl group; alternatively, a n-hexyl group;alternatively, a n-heptyl group; alternatively, a n-octyl group; oralternatively, or a n-dodecyl group.

R¹ can be a cycloalkyl group in certain aspects of this invention. Thus,R¹ can be a C₃ to C₁₈ cycloalkyl group, a C₄ to C₁₂ cycloalkyl group, aC₄ to C₁₀ cycloalkyl group, or a C₅ to C₈ cycloalkyl group. Accordingly,in some aspects, R¹ can be a cyclobutyl group, a cyclopentyl group, acyclohexyl group, a cycloheptyl group, or a cyclooctyl group;alternatively, a cyclobutyl group; alternatively, a cyclopentyl group;alternatively, a cyclohexyl group; alternatively, a cycloheptyl group;or alternatively, a cyclooctyl group.

In accordance with another aspect of this invention, any alkyl groupdisclosed herein (cycloalkyl, linear alkyl, or branched alkyl) can besubstituted with one or more substituents. Each non-hydrogensubstituent(s) for the substituted alkyl group independently can be a C₁to C₁₈ hydrocarbyl group; alternatively, a C₁ to C₈ hydrocarbyl group;or alternatively, a C₁ to C₆ hydrocarbyl group. Thus, the hydrocarbylsubstituent can be a benzyl group, a phenyl group, a tolyl group, or axylyl group, and the like, and, therefore, R¹ can be, for instance, aphenyl-substituted alkyl group. Additionally, the hydrocarbylsubstituent can be a C₁ to C₆ linear or branched alkyl group and,therefore, R¹ can be, for instance, an alkyl-substituted cycloalkylgroup, such as a methylcyclohexyl group.

An illustrative non-hydrocarbon substituent that can be present on anyalkyl group disclosed herein (cycloalkyl, linear alkyl, or branchedalkyl) is a hydroxy group (—OH group). Thus, R¹ can be a methyl alcoholor methanol group (—CH₂OH), an ethyl alcohol or ethanol group(—CH₂CH₂OH), a propanol group, a butanol group, a pentanol group, ahexanol group, and so forth.

Referring now to R² in formula (I), R² can be any C₁ to C₁₈ substitutedor unsubstituted, cycloalkyl group or linear or branched alkyl groupdisclosed herein for R¹. Thus, for example, R² can be any cycloalkylgroup, linear alkyl group, or branched alkyl group disclosed herein, andfurther, R² can be unsubstituted, or can be substituted with anysuitable substituent or any substituent disclosed herein, any suitablenumber of substituents, and at any suitable position(s) that conforms tothe rules of chemical valence.

In aspects where the sulfide compound is asymmetrical, the sulfidecompound can be methyl ethyl sulfide, methyl iso-propyl sulfide, methyldodecyl sulfide, ethyl octyl sulfide, n-pentyl n-heptyl sulfide, and thelike, as well as any combination thereof. In certain aspects, thesulfide compound can be methyl ethyl sulfide. In aspects where thesulfide compound is symmetrical, the sulfide compound can be dimethylsulfide, diethyl sulfide, di-n-propyl sulfide, di-iso-propyl sulfide,di-n-butyl sulfide, di-n-pentyl sulfide, di-n-hexyl sulfide, di-n-heptylsulfide, di-n-octyl sulfide, di-n-dodecyl sulfide, and the like, as wellas any combination thereof. In certain aspects, the sulfide compound canbe dimethyl sulfide.

Certain aspects of the processes disclosed herein may be applicable tosulfide compounds having particular characteristics, e.g., molecularweight, polarity, boiling point, etc. For instance, it can be beneficialfor the sulfide compound to be a liquid (not a solid) and to remain inthe liquid state at a particular set of process conditions, such as atstandard temperature and pressure (STP, 1 atm and 20° C.). Thus, sulfidecompounds suitable for the processes disclosed herein can be a liquid atSTP, and beneficially remain a liquid at 0° C. and 2 atm, and/or remaina liquid at −10° C. and 2 atm. While not limited thereto, the sulfidecompound can have a normal boiling point (at 1 atm) of at least about30° C., at least about 50° C., at least about 70° C., or at least about90° C. Additionally or alternatively, the sulfide compound can have anormal boiling point within 100° C., within 50° C., within 30° C., orwithin 10° C., of that of carbon disulfide (which has a normal boilingpoint of ˜46-47° C.).

Alkanolamines

Aspects of this invention are directed to processes to purify a productstream containing a sulfide compound. Such processes can comprisecontacting the product stream with any suitable alkanolamine to convertat least a portion of CS₂ in the product stream to a higher boilingpoint product. For instance, the alkanolamine can react with CS₂ presentin the product stream and convert the CS₂ to a higher boiling pointproduct, which can be more readily removed or separated from the productstream, such as via distillation. Significantly, the reactivity of thealkanolamine can be relatively low with respect to the sulfide compoundas compared to its reactivity with carbon disulfide, such that thealkanolamine can preferentially react with trace amounts of carbondisulfide even in the presence of a large excess of the sulfidecompound. In some aspects, the alkanolamine can be selected such that itdoes not react with the particular sulfide compound in the productstream.

Alkanolamines encompassed herein include compounds having both a hydroxygroup and an amine group. The alkanolamine can be a C₁ to C₁₈alkanolamine; alternatively, a C₂ to C₁₈ alkanolamine; alternatively, aC₁ to C₁₂ alkanolamine; alternatively, a C₂ to C₁₂ alkanolamine;alternatively, a C₂ to C₈ alkanolamine; or alternatively, a C₂ to C₆alkanolamine. In one aspect, the alkanolamine can be a monoalkanolamine(one hydroxy group), illustrative and non-limiting examples of which caninclude methanolamine, ethanolamine, n-propanolamine,n-isopropanolamine, n-butanolamine, isobutanolamine, and the like, aswell as combinations thereof. In another aspect, the alkanolamine can bea dialkanolamine (two hydroxy groups), illustrative and non-limitingexamples of which can include diethanolamine, diisopropanolamine, andthe like, or a combination thereof. In yet another aspect, thealkanolamine can be a trialkanolamine (three hydroxy groups), anon-limiting example of which is triethanolamine. Combinations ofalkanolamines can be used in the disclosed processes, such as a mixtureof a monoalkanolamine and a dialkanolamine, a mixture of two differentmonoalkanolamines, and so forth.

The amine group in the alkanolamine can be a primary amine group, asecondary amine group, or a tertiary amine group. In particular aspectsof this invention, the alkanolamine contains a primary amine. Thealkanolamine can be linear or branched, and substituted orunsubstituted, as would be recognized by a skilled artisan.

Additionally, the alkanolamine can contain, in some aspects, aheteroatom-containing linking group between the amine and hydroxygroup(s). For example, the heteroatom can be oxygen or sulfur, and thusthe heteroatom-containing linking group can be an ether or thioether.This is illustrated by the representative alkanolamine shownbelow—2-(2-aminoethoxy)ethanol—which contains an ether group between theamine and hydroxy group.

Other suitable heteroatom-containing linking groups are alsocontemplated herein, wherein the linking group can comprise any linkinggroup formed by substituting one or more carbon atoms of any hydrocarbonlinking group (e.g., C₂ to C₁₈) disclosed herein with one moreheteroatoms. Heteroatomic linking groups can be linear or branched, andsubstituted or unsubstituted, as described above in relation to R¹ andR² of the sulfide compound.

Another non-limiting class of alkanolamines suitable for the processescontemplated herein includes β-hydroxy amines, according to formula(II):

In certain aspects of the processes contemplated herein, β-hydroxyamines can be particularly reactive with carbon disulfide in a productstream due to their ability to form stable cyclic byproducts throughreactions with carbon disulfide that can be effectively irreversible.Without being bound by theory, such aspects can convert undesired carbonsulfide in the product stream to stable byproducts that can be moreeasily removed from the product stream. In certain aspects, β-hydroxyamines of formula (II) can produce heterocyclic products byincorporating the relatively reactive carbon of the carbon disulfideinto a 5-membered heterocyclic ring, as well as other reaction productssuch as those disclosed herein (e.g., H₂S, cysteamine, etc.).

In formula (II) above, R³-R⁶ independently can be H or a C₁ to C₁₂ alkylgroup; alternatively, H or a C₁ to C₆ alkyl group; alternatively, H or aC₂ to C₁₂ alkyl group; alternatively, H or a C₂ to C₆ alkyl group; oralternatively, H or a C₁ to C₄ alkyl group. Thus, in some aspects, R³-R⁶in formula (II) independently can be H, a methyl group, an ethyl group,a propyl group, a butyl group, a pentyl group, or a hexyl group.

Similar to the sulfide compounds, suitable alkanolamines for theprocesses disclosed herein can have particular beneficialcharacteristics, including reactivity with CS₂, the ability to formcertain higher boiling point products, polarity, boiling point, etc. Forinstance, it can be beneficial for the alkanolamine to be a liquid (nota solid) and to remain in the liquid state at a particular set ofprocess conditions, such as at standard temperature and pressure (STP, 1atm and 20° C.). Thus, alkanolamines suitable for the processesdisclosed herein can be a liquid at STP, and beneficially remain aliquid at 0° C. and 2 atm, and/or remain a liquid at −10° C. and 2 atm.

EXAMPLES

The invention is further illustrated by the following examples, whichare not to be construed in any way as imposing limitations to the scopeof this invention. Various other aspects, embodiments, modifications,and equivalents thereof which, after reading the description herein, cansuggest themselves to one of ordinary skill in the art without departingfrom the spirit of the present invention or the scope of the appendedclaims.

A gas chromatography (GC) method was used to determine the ppm (byweight) of carbon disulfide. Samples were analyzed using a SulfurChemiluminescence Detector (SCD) equipped with a DB-1 column (60 m×320rpm×1 μm). The initial temperature was set to 40° C. for 4 minutes, thenramped to 60° C. at 5° C./min, then to 170° C. at 30° C./min. It wasfound that a sulfur specific detector was necessary for CS₂ levels ofless than 50 ppm in dimethyl sulfide; a FID detector was inadequate.

Comparative Example

The comparative example utilized conventional distillation processes forpurifying a product stream containing dimethyl sulfide. Two distillationcolumns were used. Columns T-3 and T-2 were packed columns: T-3 had 63theoretical stages and T-2 had 40 theoretical stages, and about 75 and50 feet of packing, respectively. The overhead distillate from columnT-3 was the feed to column T-2. Tables I-II summarize the conditions inColumn T-2 and Column T-3, respectively, and results of the comparativedistillation process taken at roughly six-hour intervals over the courseof about ten days. As is shown, the temperature and pressure were variedin an effort to improve the separation of the carbon disulfide impurityfrom dimethyl sulfide.

Referring first to Table II and comparing the amount of CS₂ in theoverhead (average ˜1000 ppm) versus in the kettle (average ˜4000), itcan be concluded that while a significant amount of CS₂ can be removedin column T-3, it is very difficult to consistently produce an overheadstream containing less than 1000 ppm by weight of CS₂.

Referring now to Table I and comparing the amount of CS₂ in the overheadversus in the kettle, it can be concluded that the amount of CS₂ removedin column T-2 is highly variable, and in some cases, distillation incolumn T-2 was completely ineffective at reducing the amount of CS₂.Significantly, there was no data in these experiments to indicate that apurified stream containing less than 250 ppm by weight of CS₂ (or lessthan 100 ppm) could possibly be achieved using distillation.

In sum, distillation was not able to efficiently separate CS₂ from adimethyl sulfide product stream in order to achieve a high puritydimethyl sulfide stream, for example, with CS₂ levels of much less than500 ppm, such as 250 ppm or less, 100 ppm or less, or 20 ppm or less.

Examples 1-12

Examples 1-12 were conducted with samples of dimethyl sulfide havingknown concentrations of CS₂. In each experiment, an amount of dimethylsulfide “product stream” was mixed with an alkanolamine, and theconcentration of CS₂ was monitored for up to 150 minutes. Variousloadings of the alkanolamine were examined, as well as variouscontacting temperatures. It was observed that the conversion of CS₂occurred quickly in most cases, proceeding either to completely removeCS₂ from the product stream, or stabilize within about 30 minutes.

Table III summarizes the results of the conversion reactions of Examples1-12, and shows the starting concentrations of CS₂ around 2000-2700 ppm(by weight), and the final concentration of CS₂ after a set period oftime. Surprisingly, the molar ratio of the alkanolamine:CS₂ that allowedthe conversion to proceed quickly to completion in each example wasgreater than 1:1. Thus, a simple stoichiometric amount of alkanolaminebased on the amount of CS₂ present in the sulfide product stream may notbe sufficient in all cases to convert the CS₂ to a higher boiling pointproduct, thereby removing it from the product stream. In Example 1, adimethyl sulfide product stream having a CS₂ concentration of 2088 ppmwas mixed with 0.3 wt. % monoethanolamine (based on the weight of thedimethyl sulfide product stream), or an alkanolamine:CS₂ molar ratio of1.8:1. While the amount of CS₂ present in the mixture decreased over thecourse of the reaction, the final concentration of CS₂ in the mixturewas significant even after 150 minutes. In comparison, increasing theamount of monoethanolamine to 0.5 wt. % (Example 2) reduced the amountof CS₂ drastically, to 97 ppm after 120 minutes. At 36° C., Example 3used monoethanolamine at a concentration of 0.7 wt. % and completelyconverted the CS₂ present in the mixture within less than 30 minutes.

Examples 4-7 were conducted at 36° C. and produced similar results toExamples 1-3. Notably, the amount of monoethanolamine needed forcomplete conversion of the CS₂ appears to scale with the amount of CS₂present, despite alkanolamine:CS₂ ratios of less than about 3:1 notfully converting the CS₂ present in the product mixture to higherboiling point products. Particularly, Example 4 used a loading of 0.3wt. %, and the CS₂ level dropped to 847 ppm after 30 minutes, Example 5used a loading of 0.5 wt. %, and the CS₂ level dropped to 375 ppm after60 minutes, while Example 6 used a loading of 0.71 wt. %, and almostconverted all the CS₂ within 30 minutes, leaving only a small amount ofCS₂ remaining in the product mixture (46 ppm). In contrast, increasingthe monoethanolamine loading to 0.85 wt. % (Example 7) resulted in thecomplete conversion of CS₂ in less than 5 minutes. From these examples,it appears that increasing amounts of CS₂ can be removed from a productstream by using increasing amounts of alkanolamine proportional to theamount of CS₂ present in the initial sulfide product stream. Moreover,CS₂ conversion occurs very quickly when an adequate amount ofalkanolamine is present in the product mixture, either at roomtemperature or at elevated temperatures.

Examples 8-10 demonstrate that diluting the alkanolamine does notadversely affect the conversion of CS₂ after 30 minutes, and similarconversion rates and speeds are observed. Surprisingly, for Examples9-10, the CS₂ level dropped to zero after only 5 minutes. Examples 11-12examine the effect of other alkanolamines in converting the CS₂ tohigher boiling point products after 30 minutes. As is shown in TableIII, 1-amino-2-propanol and diethanolamine were effective in convertingthe CS₂, at alkanoamine:CS₂ ratios similar to those used forethanolamine in Examples 1-10.

Examples 13-20

Examples 13-20 were performed as bench scale purifications of a dimethylsulfide product stream comprising CS₂ to demonstrate that the conversionof CS₂ in the contacting step could effectively prevent any amount ofCS₂ from being transferred to the overhead (O/H) purified productstream. Examples 13-20 also examine alternate alkanolamines that can beused during the contacting step. Results are summarized in Table IV. A500-mL jacketed distillation kettle was equipped with an 8-inchdistillation column packed with structured metal packing. To this wasattached a condenser and overhead sample collection flask. The kettlewas heated using glycol heated to 45° C. and a reflux ratio of 5:5 wasused. The exact amount of CS₂ present initially in the dimethyl sulfideproduct stream was not analyzed, but was in the 2000-3000 ppm range.

Surprisingly, alkanolamines that are not β-hydroxy amines weresuccessful in completely converting the CS₂ to higher boiling pointproducts. Without being bound by theory, these alternate β-hydroxyamines also may form alternate higher boiling point products by reactionwith CS₂, which are easily separated from a target sulfide compound(dimethyl sulfide) during distillation. Moreover, in each of Examples13-20 where the conversion of CS₂ during the contacting step wascomplete, no amount of CS₂ (0 ppm) was observed in the purified dimethylsulfide stream. Example 13 demonstrated that ethanolamine wasparticularly effective, requiring a loading of 0.5 wt. % (based on theweight of the initial dimethyl sulfide product stream) to convert all ofthe CS₂ present in the dimethyl sulfide stream. Other alkanolamines alsowere shown to be effective in the conversion of CS₂ to higher boilingpoint products, which can then be easily separated from dimethyl sulfideby conventional distillation.

TABLE I Column T-2 Kettle Kettle Overhead Overhead Product ProductReboiler Column Column H₂O, CS₂, H₂O, CS₂, stream, stream Reflux,Pressure, steam, Temperature Temperature Entry ppm ppm ppm ppm gpm ° C.gpm psig lb/hr (bottom, ° C.) (top, ° C.) A1 181 1708 243 1764 3.5 62 1314 1100 66 67 A2 33 1669 36 1901 2.5 56 13 9 1100 60 60 A3 33 1547 371625 2.4 54 13 8 1100 59 58 A4 21 782 38 1295 1.0 50 14 6 1100 57 56 A541 713 39 1179 1.0 49 14 5 1100 56 54 A6 29 606 53 970 1.0 52 15 6 110057 57 A7 28 507 40 969 1.0 50 14 6 1100 57 56 A8 26 577 45 1079 1.0 4914 5 1100 56 54 A9 40 647 38 1118 1.0 49 14 5 1100 56 55 A10 38 581 511052 1.0 51 14 6 1100 57 56 A11 51 572 46 1128 1.0 51 14 5 1100 57 57A12 61 591 50 1106 1.0 49 14 5 1100 55 54 A13 24 605 38 1118 1.0 49 14 61100 55 54 A14 35 581 37 1115 1.0 51 16 6 1245 57 57 A15 55 724 63 10191.0 53 18 7 1445 59 58 A16 32 699 39 936 1.0 57 19 6 1440 64 59 A17 25744 39 1015 1.0 57 18 6 1408 63 59 A18 54 739 50 1009 1.0 54 19 7 140761 58 A19 53 720 60 1007 1.0 56 19 6 1411 63 59 A20 56 705 52 1046 1.056 19 7 1425 62 59 A21 46 695 49 976 1.0 56 19 7 1425 63 59 A22 35 91657 795 1.0 59 14 39 1350 65 60 A23 31 1359 65 584 1.0 81 16 34 1350 8788 A24 38 1524 45 615 1.0 78 14 41 1350 84 85 A25 58 1747 44 635 1.0 8215 39 1350 96 90 A26 25 1640 721 362 1.0 81 15 37 1350 95 89 A27 1201295 110 546 1.0 80 15 36 1350 94 88 A28 41 1787 84 532 1.0 79 14 511350 93 87 A29 64 1715 85 548 1.0 89 14 49 1350 103 97 A30 40 1913 77619 1.0 88 14 49 1350 102 96 A31 50 2130 83 701 1.0 88 14 50 1350 101 96A32 232 1434 170 559 1.0 88 15 48 1350 101 96 A33 47 2008 87 615 1.0 8815 48 1350 102 95 A34 73 2154 73 661 1.0 87 14 49 1350 101 95 A35 1661520 253 444 1.0 88 15 49 1350 101 96 A36 292 1649 344 633 1.0 88 15 491350 102 96 A37 66 2259 45 601 1.0 88 14 48 1350 102 96 A38 116 2427 84724 1.0 87 14 49 1350 101 95 A39 40 1599 90 786 1.0 87 3 61 340 101 95A40 60 1344 75 765 1.0 94 2 63 478 108 103 A41 60 1474 86 845 1.0 94 652 686 108 102 A42 29 2052 84 943 1.0 89 11 52 1051 103 97 A43 65 224752 825 1.0 89 12 52 1195 103 97 A44 56 2434 53 829 1.0 89 14 52 1309 10397

TABLE II Column T-3. Kettle Kettle Overhead Overhead Product ProductReboiler Column Column H₂O, CS₂, H₂O, CS₂, stream, stream Reflux,Pressure, steam, Temperature Temperature Entry ppm ppm ppm ppm gpm ° C.gpm psig lb/hr (bottom, ° C.) (top, ° C.) B1 32 5934 94 2020 4 81 35 533000+ 101  99 B2 45 5792 27 1847 4 82 45 58 3000+ 105 104 B3 33 5507 531585 4 79 46 60 3000+ 105 104 B4 24 4425 37 1209 4 78 50 63 3000+ 108107 B5 42 4321 40 971 4 74 51 65 3000+ 108 107 B6 810 4250 22 902 4 7650 66 3000+ 109 108 B7 30 4092 28 868 4 79 49 63 3000+ 107 107 B8 334100 52 955 4 78 47 59 3000+ 105 104 B9 37 4155 37 1032 4 79 48 61 3000+106 106 B10 22 4337 26 874 4 83 50 66 3000+ 108 108 B11 0 2955 0 870 479 49 64 3000+ 108 107 B12 76 4042 32 1001 4 77 48 59 3000+ 104 104 B1323 4144 41 967 4 77 48 59 3000+ 104 104 B14 11 4062 25 1016 4 78 49 633000+ 107 107 B15 46 4108 29 954 4 79 49 63 3000+ 107 107 B16 72 4307 521048 4 77 47 61 3000+ 106 105 B17 38 4201 43 1037 4 77 48 62 3000+ 106106 B18 20 4161 38 1016 4 77 48 60 3000+ 105 104 B10 42 4437 38 937 3 8649 63 3000+ 107 107 B20 35 4531 49 924 3 84 49 63 3000+ 107 106 B21 554499 47 905 4 83 50 63 3000+ 107 106 B22 35 4344 39 952 4 78 50 65 3000+108 107 B23 30 4106 41 1002 4 78 50 65 3000+ 108 108 B24 35 4060 51 8894 78 50 65 3000+ 108 225 B25 35 4096 46 990 4 77 48 61 3000+ 106 221 B2632 4082 104 819 4 78 48 66 3000+ 109 226 B27 188 3337 443 432 4 79 49 693000+ 110 229 B28 23 3927 93 799 4 78 48 67 3000+ 109 228 B29 37 4310 68820 4 36 48 65 3000+ 108 224 B30 41 4003 124 656 4 39 43 63 3000+ 107224 B31 99 3913 76 972 4 29 40 60 3000+ 105 219 B32 48 3797 882 754 4 4042 66 3000+ 108 225 B33 56 3836 643 1029 4 42 41 65 3000+ 108 225 B34 494027 105 896 4 37 40 63 3000+ 107 223 B35 73 4002 61 1108 4 31 38 613000+ 106 221 B36 83 3688 771 750 4 42 39 66 3000+ 108 226 B37 166 3015226 725 4 42 39 66 3000+ 108 226 B38 90 3866 273 976 4 31 36 61 3000+105 220 B39 90 3772 76 1069 4 31 35 55 3000+ 102 215 B40 26 3885 44 10994 36 36 56 3000+ 103 216 B41 64 3995 73 1270 4 32 36 54 3000+ 102 213B42 50 3860 44 1221 4 30 35 52 3000+ 101 211 B43 30 3790 48 1242 4 34 3657 3000+ 103 217 B44 57 4032 49 1205 4 38 38 63 3000+ 107 223 B45 604025 55 1135 4 31 38 61 3000+ 106 221

TABLE III Examples 1-12. Temperature DMS AA AA Initial CS₂ Final CS₂Example (° C.) (g) Alkanolamine (AA) (wt. %) (mmol) (ppmw) (ppmw) AA:CS₂1 20 50 ethanolamine 0.30 2.46 2088 687 1.8 2 20 202 ethanolamine 0.5016.37 2057 97 3.0 3 36 — ethanolamine 0.70 — 2321 0 — 4 36 —ethanolamine 0.30 — 2046 847 — 5 36 92 ethanolamine 0.50 7.53 2353 3752.6 6 36 99 ethanolamine 0.71 11.46 2664 46 3.3 7 36 130 ethanolamine0.85 18.01 2664 0 4.0 8 20 100 ethanolamine (85% in methanol) 0.51 8.222204 41 2.9 9 20 100 ethanolamine (85% in methanol) 0.77 12.13 2363 04.0 10 20 100 ethanolamine (50% in methanol) 0.70 10.92 2204 0 3.9 11 36153 1-amino-2-propanol 0.80 11.60 2664 134 2.3 12 36 73 diethanolamine0.55 5.33 2235 942 2.6

TABLE IV Examples 13-20. Alkanol- amine Initial ppm ppm Loading CS₂ CS₂CS₂ Example Chemical name (wt %) (ppm) kettle O/H 13 monoethanolamine0.5 2000-3000    0    0 14 diisopropanolamine 0.7 2000-3000  292  820 153-amino-1-propanol 0.5 2000-3000    0    0 16 1-amino-2-propanol 0.52000-3000    0    0 17 2-(2-aminoethoxy)ethanol 0.6 2000-3000    0    018 1-amino-2-butanol 0.6 2000-3000  304    0 19 ethylene diamine 0.52000-3000    0    0 20 methyldiethanolamine 1.0 2000-3000 2319 3016

The invention is described above with reference to numerous aspects andembodiments, and specific examples. Many variations will suggestthemselves to those skilled in the art in light of the above detaileddescription. All such obvious variations are within the full intendedscope of the appended claims. Other aspects of the invention caninclude, but are not limited to, the following (aspects typically aredescribed as “comprising” but, alternatively, can “consist essentiallyof” or “consist of” unless specifically stated otherwise):

Aspect 1. A process to purify a product stream containing a sulfidecompound and CS₂, the process comprising:

(i) contacting the product stream with an alkanolamine to convert atleast a portion of the CS₂ to a higher boiling point product; and

(ii) removing at least a portion of the higher boiling point productfrom the product stream to form a purified sulfide stream.

Aspect 2. The process defined in aspect 1, wherein the sulfide compoundhas formula (I): R¹—S—R² (I); wherein:

R¹ and R² independently are a C₁ to C₁₈ substituted or unsubstituted,cycloalkyl group or linear or branched alkyl group.

Aspect 3. The process defined in aspect 2, wherein R¹ and R²independently are a branched alkyl group.

Aspect 4. The process defined in aspect 2, wherein R¹ and R²independently are a linear alkyl group.

Aspect 5. The process defined in aspect 2, wherein R¹ and R²independently are a substituted alkyl group (e.g., a phenyl-substitutedalkyl group).

Aspect 6. The process defined in any one of aspects 2-5, wherein R¹ andR² independently are a C₁ to C₁₂ alkyl group.

Aspect 7. The process defined in aspect 2, wherein R¹ and R²independently are a methyl group, an ethyl group, a propyl group, abutyl group, a pentyl group, a hexyl group, a heptyl group, an octylgroup, a nonyl group, a decyl group, a undecyl group, a dodecyl group, atridecyl group, a tetradecyl group, a pentadecyl group, a hexadecylgroup, a heptadecyl group, or an octadecyl group.

Aspect 8. The process defined in aspect 2, wherein R¹ and R²independently are a methyl group, an ethyl group, a n-propyl group, aniso-propyl group, a n-butyl group, an iso-butyl group, a sec-butylgroup, a tert-butyl group, a n-pentyl group, an iso-pentyl group, asec-pentyl group, a neopentyl group, or a tert-amyl group.

Aspect 9. The process defined in aspect 2, wherein R¹ and R²independently are a methyl group or an ethyl group.

Aspect 10. The process defined in any one of aspects 2-9, wherein R¹ andR² are different.

Aspect 11. The process defined in any one of aspects 2-9, wherein R¹ andR² are the same.

Aspect 12. The process defined in aspect 1 or 2, wherein the sulfidecompound is methyl ethyl sulfide, methyl iso-propyl sulfide, methyldodecyl sulfide, ethyl octyl sulfide, n-pentyl n-heptyl sulfide, or anycombination thereof.

Aspect 13. The process defined in aspect 1 or 2, wherein the sulfidecompound is methyl ethyl sulfide.

Aspect 14. The process defined in aspect 1 or 2, wherein the sulfidecompound is dimethyl sulfide, diethyl sulfide, di-n-propyl sulfide,di-iso-propyl sulfide, di-n-butyl sulfide, di-n-pentyl sulfide,di-n-hexyl sulfide, di-n-heptyl sulfide, di-n-octyl sulfide,di-n-dodecyl sulfide, or any combination thereof.

Aspect 15. The process defined in aspect 1 or 2, wherein the sulfidecompound is dimethyl sulfide.

Aspect 16. The process defined in any one of aspects 1-15, wherein thesulfide compound is a liquid at any set of conditions disclosed herein(e.g., standard temperature and pressure, 0° C. and 2 atm, or −10° C.and 2 atm).

Aspect 17. The process defined in any one of aspects 1-16, wherein theproduct stream comprises any wt. % of the sulfide compound disclosedherein, e.g., at least about 95 wt. %, at least about 99 wt. %, fromabout 95 wt. % to about 99.99 wt. %, or from about 99 wt. % to about99.9 wt. %.

Aspect 18. The process defined in any one of aspects 1-17, wherein theproduct stream comprises any minimum amount of CS₂ disclosed herein,e.g., a minimum of about 250 ppm, a minimum of about 500 ppm, or aminimum of about 1000 ppm (by weight).

Aspect 19. The process defined in any one of aspects 1-18, wherein theproduct stream comprises an amount of CS₂ in any range disclosed herein,e.g., from about 250 to about 5000 ppm, from about 500 ppm to about10,000 ppm, from about 1000 to 5000 ppm, or from about 2000 to about4000 ppm (by weight).

Aspect 20. The process defined in any one of aspects 1-19, wherein theproduct stream further comprises an amount of H₂S in any range disclosedherein, e.g., from about 1 to about 100 ppm, from about 100 ppm to about250 ppm, or from about 250 to about 1000 ppm (by weight).

Aspect 21. The process defined in any one of aspects 1-20, wherein thealkanolamine is a C₁ to C₁₂ alkanolamine, or a C₂ to C₆ alkanolamine.

Aspect 22. The process defined in any one of aspects 1-21, wherein thealkanolamine is a monoalkanolamine (e.g., methanolamine, ethanolamine,n-propanolamine, isopropanolamine, n-butanolamine, isobutanolamine, orany combination thereof); alternatively, a dialkanolamine (e.g.,diethanolamine, diisopropanolamine, or a combination thereof); oralternatively, a trialkanolamine (e.g., triethanolamine).

Aspect 23. The process defined in any one of aspects 1-22, wherein thealkanolamine contains a primary amine; alternatively, a secondary amine;or alternatively, a tertiary amine.

Aspect 24. The process defined in any one of aspects 1-23, wherein thealkanolamine comprises a heteroatom-containing linking group between thehydroxy and the amine group.

Aspect 25. The process defined in any one of aspects 1-21, wherein thealkanolamine is a β-hydroxy amine having the formula (II):

wherein R³, R⁴, R⁵, and R⁶ independently are H or a C₁ to C₁₂ alkylgroup.

Aspect 26. The process defined in any one of aspects 1-25, wherein thealkanolamine is a liquid at standard temperature and pressure (20° C.and 1 atm).

Aspect 27. The process defined in any one of aspects 1-26, wherein thealkanolamine does not react with the sulfide compound.

Aspect 28. The process defined in any one of aspects 1-27, wherein instep (i), the product stream is contacted with the alkanolamine in adiluent.

Aspect 29. The process defined in aspect 28, wherein the diluentcomprises a C₁ to C₃ alcohol.

Aspect 30. The process defined in aspect 28 or 29, wherein a weightratio of alkanolamine:diluent is in any suitable range or any rangedisclosed herein, e.g., from about 95:5 to about 25:75, from about 85:15to about 50:50, or from about 90:10 to about 70:30.

Aspect 31. The process defined in any one of aspects 1-30, wherein step(i) is conducted at a temperature in any suitable range or any rangedisclosed herein, e.g., from about 15° C. to about 85° C., from about20° C. to about 70° C., or from about 25° C. to about 60° C.

Aspect 32. The process defined in any one of aspects 1-31, wherein step(i) is conducted at a pressure in any suitable range or any rangedisclosed herein, e.g., from ambient to about 100 psig (689 kPag), orfrom about 5 to about 60 psig (34 to 414 kPag).

Aspect 33. The process defined in any one of aspects 1-32, wherein instep (i), a molar ratio of alkanolamine:CS₂ is in any suitable range orany range disclosed herein, e.g., from about 1:1 to about 20:1, fromabout 1.5:1 to about 10:1, or from about 2:1 to about 6:1.

Aspect 34. The process defined in any one of aspects 1-33, wherein instep (i), an amount of the alkanolamine added to the product stream isin any suitable range or any range disclosed herein, e.g., from about0.1 to about 2 wt. %, from about 0.2 to about 1 wt. %, or from about 0.4to about 1.5 wt. %, based on the weight of the product stream.

Aspect 35. The process defined in any one of aspects 1-34, wherein step(i) is conducted for a time period in any suitable range or any rangedisclosed herein, e.g., from about 1 min to about 24 hr, from about 2min to about 2 hr, from about 2 min to about 30 min, or from about 5 minto about 1 hr.

Aspect 36. The process defined in any one of aspects 1-35, wherein instep (i), contacting the product stream with the alkanolamine comprisesagitating a mixture of the product stream and the alkanolamine.

Aspect 37. The process defined in any one of aspects 1-36, wherein instep (i), any percentage amount disclosed herein of the CS₂ is convertedto the higher boiling point product, e.g., at least about 50 wt. %, atleast about 80 wt. %, from about 60 wt. % to about 99.99 wt. %, or fromabout 90 to about 99.99 wt. %.

Aspect 38. The process defined in any one of aspects 1-37, wherein thehigher boiling point product comprises a heterocyclic organic compound,e.g., with oxygen, nitrogen, sulfur, or any combination thereof, in thering.

Aspect 39. The process defined in any one of aspects 1-38, wherein thehigher boiling point product has a boiling point at least 30° C. greaterthan the boiling point of the sulfide compound.

Aspect 40. The process defined in any one of aspects 1-39, wherein thehigher boiling point product is a liquid at standard conditions or anyconditions disclosed herein (e.g., standard temperature and pressure, 0°C. at 2 atm, or −10° C. at 2 atm).

Aspect 41. The process defined in any one of aspects 1-40, wherein instep (ii), the higher boiling point product is removed from the productstream using any suitable technique or any technique disclosed herein,e.g., extraction, filtration, evaporation, distillation, or anycombination thereof, to form the purified sulfide stream.

Aspect 42. The process defined in any one of aspects 1-41, wherein instep (ii), the higher boiling point product is removed from the productstream using distillation to form the purified sulfide stream.

Aspect 43. The process defined in aspect 42, wherein distillation isperformed at any suitable conditions, e.g., a pressure from ambient toabout 100 psig and a temperature from about 35° C. to about 125° C.

Aspect 44. The process defined in any one of aspects 1-43, wherein instep (ii), any percentage amount disclosed herein of the higher boilingpoint product is removed from the product stream, e.g., at least about50 wt. %, at least about 80 wt. %, from about 60 to about 99.99 wt. %,or from about 90 to about 99.99 wt. %.

Aspect 45. The process defined in any one of aspects 1-44, wherein thepurified sulfide stream comprises any wt. % of the sulfide compounddisclosed herein, e.g., at least about 99.9 wt. %, at least about 99.99wt. %, or at least about 99.995 wt. %.

Aspect 46. The process defined in any one of aspects 1-45, wherein thepurified sulfide stream comprises an amount of CS₂ in any rangedisclosed herein, e.g. a maximum of about 200 ppm, a maximum of about100 ppm, a maximum of about 75 ppm, a maximum of about 25 ppm, a maximumof about 10 ppm, a maximum of about 1 ppm, in a range from about 1 toabout 100 ppm, or in a range from about 1 to about 50 ppm (by weight).

Aspect 47. The process defined in any one of aspects 1-46, wherein anypercentage amount disclosed herein of the CS₂ is converted to a higherboiling point product, e.g., at least about 90 wt. %, at least about 95wt. %, from about 90 to about 99.9 wt. %, or from about 98 to about99.99 wt. %.

Aspect 48. The process defined in any one of aspects 1-47, wherein priorto step (i), a ratio of a ppm concentration of CS₂ present in theproduct stream to the ppm concentration of CS₂ present in the purifiedsulfide stream is in any range disclosed herein, e.g., at least about10:1, at least about 25:1, at least about 100:1, or at least about500:1.

Aspect 49. The process defined in any one of aspects 1-48, furthercomprising the steps of:

(a) determining a concentration of the CS₂ in the product stream; and

(b) adjusting an amount of the alkanolamine contacted with the productstream based on the concentration of the CS₂ in the product stream.

Aspect 50. The process defined in any one of aspects 1-49, furthercomprising the steps of:

(A) determining a concentration of the CS₂ in the purified sulfidestream; and

(B) adjusting an amount of the alkanolamine contacted with the productstream based on the concentration of the CS₂ in the purified sulfidestream.

Aspect 51. A mercaptan and sulfide production system comprising (a) amercaptan synthesis unit configured to produce a reaction mixturecontaining a mercaptan compound and a sulfide compound from an alcoholfeed stream and a H₂S feed stream (e.g., producing methyl mercaptan anddimethyl sulfide from methanol and H₂S, or producing ethyl mercaptan anddiethyl sulfide from ethanol and H₂S, etc.), the mercaptan synthesisunit comprising a fixed bed catalytic flow reactor; (b) a productpurification and fractionation unit configured to isolate a mercaptanproduct stream and a sulfide product stream (comprising the sulfidecompound and CS₂) from the reaction mixture, the product purificationand fractionating unit comprising one or more separators; and (c) adistillation tower configured to separate at least a portion of a higherboiling point product from the sulfide compound in the sulfide productstream to form a purified sulfide stream containing 100 ppm or less CS₂exiting the top of the distillation tower.

Aspect 52. The system defined in aspect 51, wherein the system furthercomprises (d) a first inlet for introducing the sulfide product streamand a second inlet for introducing an alkanolamine into the distillationtower, wherein the distillation tower is further configured forcontacting the alkanolamine with the sulfide product stream to convertat least a portion of the CS₂ in the sulfide product stream to thehigher boiling point product.

Aspect 53. The system defined in aspect 51, wherein the system furthercomprises a (d) distillation tower inlet configured to introduce a mixedstream of an alkanolamine and the sulfide product stream into thedistillation tower, wherein at least a portion of the CS₂ in the sulfideproduct stream is converted to the higher boiling point product.

Aspect 54. The system defined in any one of aspects 52-53, furthercomprising (e) an analytical system (e.g., a sulfur chemiluminescencedetector) configured to measure a concentration of CS₂ in the purifiedsulfide stream exiting the top of the distillation tower; and (f) afeedback controller configured to adjust an amount of the alkanolamineintroduced into the distillation tower based on the concentration of CS₂measured by the analytical system (e.g., the amount of CS₂ measured inthe purified sulfide stream is compared to a set point concentration ofCS₂, and when the measured concentration of CS₂ is greater than the setpoint concentration of CS₂, more alkanolamine is added).

Aspect 55. The system defined in aspect 54, wherein (e) the analyticalsystem is further configured to measure a concentration of CS₂ in thesulfide product stream; and (f) the feedback controller is furtherconfigured to maintain a molar feed ratio of alkanolamine:CS₂ (molarfeed rate of alkanolamine introduced directly into the tower or in themixed stream introduced into the tower divided by the molar feed rate ofCS₂ in the sulfide product stream introduced directly into the tower orin the mixed stream introduced into the tower) in any suitable range orany range disclosed herein, e.g., from about 1:1 to about 20:1, fromabout 1.5:1 to about 10:1, or from about 2:1 to about 6:1.

Aspect 56. The system defined in any one of aspects 52-55, wherein thealkanolamine is defined in any one of aspects 21-27 (e.g.,ethanolamine).

Aspect 57. The system defined in any one of aspects 51-56, wherein thesulfide compound is defined in any one of aspects 2-16 (e.g., dimethylsulfide).

Aspect 58. The system defined in any one of aspects 51-57, wherein thesulfide product stream contains less than 25 ppm mercaptan compounds, orless than 5 ppm mercaptan compounds (or thiol compounds), and less than500 ppm water, or less than 200 ppm water.

We claim:
 1. A process to purify a product stream containing a sulfidecompound and CS₂, the process comprising: (i) contacting the productstream with an alkanolamine to convert at least a portion of the CS₂ toa higher boiling point product, wherein the product stream contains atleast about 80 wt. % of the sulfide compound; and (ii) removing at leasta portion of the higher boiling point product from the product stream toform a purified sulfide stream.
 2. The process of claim 1, wherein thesulfide compound has formula (I):R¹—S—R²  (I); wherein R¹ and R² independently are a C₁ to C₁₈substituted or unsubstituted, cycloalkyl group or linear or branchedalkyl group.
 3. The process of claim 2, wherein R¹ and R² independentlyare a C₁ to C₁₂ alkyl group.
 4. The process of claim 1, wherein thesulfide compound is methyl ethyl sulfide or dimethyl sulfide.
 5. Theprocess of claim 1, wherein the product stream contains: at least about99 wt. % of the sulfide compound; and at least about 500 ppm of CS₂. 6.The process of claim 1, wherein the alkanolamine is a C₂ to C₆alkanolamine.
 7. The process of claim 1, wherein the alkanolamine is amonoalkanolamine selected from methanolamine, ethanolamine,n-propanolamine, isopropanolamine, n-butanolamine, isobutanolamine, orany combination thereof.
 8. The process of claim 1, wherein thealkanolamine is a dialkanolamine or a trialkanolamine.
 9. The process ofclaim 1, wherein the alkanolamine comprises a heteroatom-containinglinking group between the hydroxy and the amine group.
 10. The processof claim 1, wherein the alkanolamine is a β-hydroxy amine having formula(II):

wherein R³, R⁴, R⁵, and R⁶ independently are H or a C₁ to C₁₂ alkylgroup.
 11. The process of claim 1, wherein the higher boiling pointproduct comprises a heterocyclic organic compound.
 12. The process ofclaim 1, wherein: a molar ratio of alkanolamine:CS₂ in step (i) is in arange from about 1.5:1 to about 10:1; and an amount of the alkanolaminecontacted with the product stream is in a range from about 0.1 wt. % toabout 2 wt. %, based on the weight of the product stream.
 13. Theprocess of claim 1, wherein in step (i): the product stream is contactedwith the alkanolamine in an alcohol diluent; and a weight ratio ofalkanolamine:diluent is in a range from about 95:5 to about 25:75. 14.The process of claim 1, wherein: at least about 95 wt. % of the CS₂ inthe product stream is converted to the higher boiling point product; andthe higher boiling point product has a boiling point at least 30° C.greater than the boiling point of the sulfide compound.
 15. The processof claim 1, wherein in step (ii), the higher boiling point product isremoved from the product stream using distillation to form the purifiedsulfide stream.
 16. The process of claim 1, wherein the purified sulfidestream contains: at least about 99.9 wt. % of the sulfide compound; andless than or equal to about 75 ppm of CS₂.
 17. The process of claim 1,wherein: the sulfide compound is dimethyl sulfide; the alkanolamine isethanolamine; a molar ratio of ethanolamine:CS₂ in step (i) is in arange from about 2:1 to about 6:1; an amount of the ethanolaminecontacted with the product stream is in a range from about 0.4 wt. % toabout 1.5 wt. %, based on the weight of the product stream; and thepurified sulfide stream contains less than or equal to about 25 ppm ofCS₂.
 18. The process of claim 1, wherein: at least about 95 wt. % of thehigher boiling point product is removed from the product stream to formthe purified sulfide stream; and a ratio of a ppm concentration of CS₂in the product stream prior to step (i) to a ppm concentration of CS₂ inthe purified sulfide stream is at least about 100:1.
 19. The process ofclaim 1, further comprising the steps of: (a) determining aconcentration of the CS₂ in the product stream; and (b) adjusting anamount of the alkanolamine contacted with the product stream based onthe concentration of the CS₂ in the product stream.
 20. The process ofclaim 1, further comprising the steps of: (A) determining aconcentration of the CS₂ in the purified sulfide stream; and (B)adjusting an amount of the alkanolamine contacted with the productstream based on the concentration of the CS₂ in the purified sulfidestream.
 21. A process to purify a product stream containing a sulfidecompound and CS₂, the process comprising: (i) contacting the productstream with an alkanolamine to convert at least a portion of the CS₂ toa higher boiling point product, wherein the product stream contains: atleast about 95 wt. % of the sulfide compound; and from about 250 ppm toabout 5000 ppm of CS₂; and (ii) removing at least a portion of thehigher boiling point product from the product stream to form a purifiedsulfide stream.
 22. The process of claim 21, wherein: the sulfidecompound is dimethyl sulfide; the alkanolamine is ethanolamine; in step(ii), the higher boiling point product is removed from the productstream using distillation to form the purified sulfide stream; and thepurified sulfide stream contains less than or equal to about 75 ppm ofCS₂.
 23. The process of claim 22, wherein: a molar ratio ofethanolamine:CS₂ in step (i) is in a range from about 1.5:1 to about10:1, and/or an amount of the ethanolamine contacted with the productstream is in a range from about 0.1 wt. % to about 2 wt. %, based on theweight of the product stream; and the purified sulfide stream containsat least about 99.9 wt. % of dimethyl sulfide and less than or equal toabout 25 ppm of CS₂.
 24. The process of claim 21, further comprising thesteps of: (a) determining a concentration of the CS₂ in the productstream; and (b) adjusting an amount of the alkanolamine contacted withthe product stream based on the concentration of the CS₂ in the productstream; or (A) determining a concentration of the CS₂ in the purifiedsulfide stream; and (B) adjusting an amount of the alkanolaminecontacted with the product stream based on the concentration of the CS₂in the purified sulfide stream; or both.
 25. The process of claim 21,wherein a ratio of the ppm concentration of CS₂ in the product streamprior to step (i) to a ppm concentration of CS₂ in the purified sulfidestream is at least about 250:1.